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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466789생성일: 2026년 10월 26일

Chloroacetic Acid → 2-Chloro-4-(methylsulfonyl)benzoic acid

https://huagongshe.com/reaction/466789

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetic AcidHCID 300—
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Sodium SulfiteHCID 24437—
반응물2-Chloro-4-(chlorosulfonyl)benzoic acidHCID 188427—
반응물Sodium BicarbonateHCID 516892—
반응물2-Chloro-4-sulfinylbenzoic acidHCID 86746215—
용매WaterHCID 962—
생성물2-Chloro-4-(methylsulfonyl)benzoic acidHCID 735863105.9%

반응 조건

온도50 °C

반응 단계

A 250 mL round bottom flask equipped with a reflux condenser, thermometer, and magnetic stirrer was charged with 9.2 g (73 mmol) of sodium sulfite, 24.6 g (292 mmol) of sodium bicarbonate and 80 mL of water. The resulting slurry was heated to 50° C., and 20.0 g (70 mmol) of 2-chloro-4-(chlorosulfonyl)benzoic acid was added over 15 minutes. After heating at 50° C. for three hours, chloroacetic acid (10.4 g, 110 mmol) and 5.7 mL (110 mmol) of 50% aqueous sodium hydroxide were added sequentially to the aqueous solution of 2-chloro-4-sulfinylbenzoic acid, and the reaction mixture heated to reflux. After heating for 19 hours, the reaction mixture was allowed to cool to ambient temperature and acidified with dilute HCl. The precipitated solids were collected by filtration, washed with dilute HCl and dried to give 17.4 g of 2-chloro-4-(methylsulfonyl)benzoic acid as a white solid. The solid was assayed at 85% purity, corresponding to an overall yield of 89%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05157150
출처 데이터셋uspto-grants-1992_10
ORD IDord-bd1ad13c0e614bd0b9b7539c51c775b6
출처 메모uspto-grants-1992_10